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. 1994 Oct;89(2-3):153-9.
doi: 10.1007/BF00225135.

Analysis of cytoplasmic and maternal effects I. A genetic model for diploid plant seeds and animals

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Analysis of cytoplasmic and maternal effects I. A genetic model for diploid plant seeds and animals

J Zhu et al. Theor Appl Genet. 1994 Oct.

Abstract

A genetic model for modified diallel crosses is proposed for estimating variance and covariance components of cytoplasmic, maternal additive and dominance effects, as well as direct additive and dominance effects. Monte Carlo simulations were conducted to compare the efficiencies of minimum norm quadratic unbiased estimation (MINQUE) methods. For both balanced and unbalanced mating designs, MINQUE (0/1), which has 0 for all the prior covariances and 1 for all the prior variances, has similar efficiency to MINQUE(θ), which has parameter values for the prior values. Unbiased estimates of variance and covariance components and their sampling variances could be obtained with MINQUE(0/1) and jackknifing. A t-test following jackknifing is applicable to test hypotheses for zero variance and covariance components. The genetic model is robust for estimating variance and covariance components under several situations of no specific effects. A MINQUE(0/1) procedure is suggested for unbiased estimation of covariance components between two traits with equal design matrices. Methods of unbiased prediction for random genetic effects are discussed. A linear unbiased prediction (LUP) method is shown to be efficient for the genetic model. An example is given for a demonstration of estimating variance and covariance components and predicting genetic effects.

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References

    1. Theor Appl Genet. 1987 Sep;74(5):571-8 - PubMed
    1. Biometrika. 1967 Jun;54(1):93-108 - PubMed
    1. Biometrics. 1966 Sep;22(3):439-52 - PubMed
    1. Theor Appl Genet. 1983 Apr;65(1):17-23 - PubMed
    1. Theor Appl Genet. 1980 May;56(3):119-31 - PubMed